Canonical Allele Identifier: CA655279729

Gene: HMGB1

Linked Data

• COSMIC: COSN16876932

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30459026_30459027insA , CM000675.2:g.30459026_30459027insA	GRCh38
NC_000013.10:g.31033163_31033164insA , CM000675.1:g.31033163_31033164insA	GRCh37
NC_000013.9:g.29931163_29931164insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341423.10:c.*2330_*2331insT MANE Select	ENSP00000345347.5:n.*2330_*2331insT
ENST00000341423.9:c.*2330_*2331insT	ENSP00000345347.5:n.*2330_*2331insT
ENST00000405805.5:c.*2330_*2331insT	ENSP00000384678.1:n.*2330_*2331insT
NM_001313892.1:c.*2330_*2331insT	NP_001300821.1:n.*2330_*2331insT
NM_001313893.1:c.*2330_*2331insT	NP_001300822.1:n.*2330_*2331insT
NM_002128.4:c.*2330_*2331insT	NP_002119.1:n.*2330_*2331insT
NM_002128.5:c.*2330_*2331insT	NP_002119.1:n.*2330_*2331insT
NM_001363661.1:c.*2551_*2552insT	NP_001350590.1:n.*2551_*2552insT
NM_002128.6:c.*2330_*2331insT	NP_002119.1:n.*2330_*2331insT
NM_002128.7:c.*2330_*2331insT MANE Select	NP_002119.1:n.*2330_*2331insT
NM_001370339.1:c.*2656_*2657insT	NP_001357268.1:n.*2656_*2657insT
NM_001370340.1:c.*2330_*2331insT	NP_001357269.1:n.*2330_*2331insT
NM_001370341.1:c.*2330_*2331insT	NP_001357270.1:n.*2330_*2331insT
NM_001313892.2:c.*2330_*2331insT	NP_001300821.1:n.*2330_*2331insT
NM_001363661.2:c.*2551_*2552insT	NP_001350590.1:n.*2551_*2552insT